Classifications

• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
  • C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
  • C08G77/04—Polysiloxanes
  • C08G77/06—Preparatory processes
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
  • C08J3/00—Processes of treating or compounding macromolecular substances
  • C08J3/02—Making solutions, dispersions, lattices or gels by other methods than by solution, emulsion or suspension polymerisation techniques
  • C08J3/03—Making solutions, dispersions, lattices or gels by other methods than by solution, emulsion or suspension polymerisation techniques in aqueous media
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
  • C08L83/00—Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon only; Compositions of derivatives of such polymers
  • C08L83/04—Polysiloxanes
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
  • C08J2383/00—Characterised by the use of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon with or without sulfur, nitrogen, oxygen, or carbon only; Derivatives of such polymers
  • C08J2383/04—Polysiloxanes

Definitions

• the present invention relates to a method of making silicone in water emulsions. Specifically, the present invention relates to a simple process of making silicone in water emulsions in which silicones polymerize by chain extension at the interior of a silicone droplet suspended in water.
• emulsion polymerization involves emulsifying a low molecular weight silicone and an anionic or cationic surfactant in a high shear inducing device.
• the silicone is polymerized by the addition of a strong acid or base, often at elevated temperatures.
• This process can yield relatively high molecular weight silicone polymer (e.g., ⁇ 900,000 mm 2 /sec) in water emulsions.
• Emulsion polymerization however, has a number of drawbacks. For instance, polymerization in the emulsion polymerization process occurs at the silicone water interface. As such, the rate of polymerization is faster with smaller particles because of the larger surface area and, thus, it is impossible to produce large particle size, high molecular weight silicone gum in water emulsions.
• emulsion polymerization involves a number of processing steps and/or materials which are disadvantageous. For instance, emulsion polymerization requires long batch times and caustic materials (strong acidic or basic catalysts which must be neutralized).
• the emulsions resulting from emulsion polymerization may have limited utilities because of the materials used in their manufacture. For instance, the anionic and cationic surfactants used in these emulsions can be irritating to the skin and they can affect the stability of products into which the emulsions are incorporated.
• a second technique for the production of s/w emulsions is mechanical emulsion.
• a silicone polymer is mechanically emulsified with a variety of surfactants and water.
• This process allows for the production of anionic, cationic, non-ionic or amphoteric emulsions having a variety of particle sizes and high silicone fractions.
• the process is more advantageous than emulsion polymerization in that the processing time is relatively short and the process does not require heating or a neutralization step.
• the present invention provides in one of its aspects a method of making a silicone in water emulsion comprising mixing materials comprising (I) a composition containing at least one polysiloxane, at least one organosilicon material that reacts with said polysiloxane by a chain extension reaction and a metal containing catalyst for said chain extension reaction, (II) at least one surfactant and (III) water to form a mixture; and emulsifying the mixture.
• the s/w emulsions produced by the process of this invention can have a wide variety of silicone volume fractions, particle sizes and molecular weights including novel materials having large volume fractions of the silicone and large particles containing high molecular weight silicone gums. Moreover, the process results in emulsions in which the particle size and the molecular weight of the silicone inside the droplets are independent parameters.
• a mixture is prepared by blending (I) a composition containing at least one polysiloxane, at least one organosilicon material that reacts with said polysiloxane by a chain extension reaction and a metal containing catalyst for said chain extension reaction, (II) at least one surfactant and (III) water.
• composition (I) containing at least one polysiloxane, at least one organosilicon material that reacts with said polysiloxane by a chain extension reaction and a metal containing catalyst for said chain extension reaction according to this invention is not critical and nearly any which cures by the chain extension reactions can be used herein.
• chain extension reactions generally involve (1) a polysiloxane which has an end group which reacts with the end group of another polysiloxane or (2) a polysiloxane having a reactive end group which is chain extended with a chain extension agent such as an silane.
• a small amount of the chain extension can occur at non-terminal sites on the polysiloxane.
• Polysiloxanes are also called silicones or organopolysiloxanes
• silicones or organopolysiloxanes are known in the art and can involve, for instance, the hydrosilylation reaction in which an Si-H reacts with an aliphatically unsaturated group in the presence of a platinum or rhodium containing catalyst.
• the reaction can involve the reaction of an Si-OH (e.g., polymers) with an alkoxy group (e.g., alkoxysilanes, silicates or alkoxysiloxanes) in the presence of a metal containing catalyst.
• the polysiloxane(s) used in the above reactions generally comprises a substantially linear polymer of the structure:
• each R and R' independently represent a hydrocarbon group having up to 20 carbon atoms such as an alkyl (e.g., methyl, ethyl, propyl or butyl), an aryl (e.g., phenyl), or the group required for the chain extension reaction described above ('reactive group', e.g., hydrogens, aliphatically unsaturated groups such as vinyl, allyl or hexenyl, hydroxys, alkoxys such as methoxy, ethoxy or propoxy, alkoxy-alkoxy, acetoxys, aminos and the like), provided that on average there is between one and two reactive groups (inclusive) per polymer, and n is a positive integer greater than one.
• a majority, more preferably >90%, and most preferably >98% of the reactive groups are end-groups, i.
• n is an integer that results in polysiloxanes with viscosities between about 1 and about 1x10 6 mm 2 /sec at 25°C.
• the polysiloxane (I) can have a small amount of branching (e.g., less than 2 mole % of the siloxane units) without affecting the invention, i.e., the polymers are 'substantially linear'.
• the R and R' groups can be substituted with, for instance, nitrogen containing groups (e.g., amino groups), epoxy groups, sulphur containing groups, silicon containing groups, oxygen containing groups and the like.
• nitrogen containing groups e.g., amino groups
• epoxy groups e.g., sulphur containing groups
• silicon containing groups e.g., silicon containing groups
• oxygen containing groups e.g., oxygen containing groups
• at least 80% of the R groups are alkyls and, more preferably, the alkyl groups are methyl groups.
• the organosilicon material that reacts with the polysiloxane by a chain extension reaction can be either a second polysiloxane or a material that acts as a chain extension agent. If the organosilicon material is polysiloxane, it too will generally have the structure described above (I). In such a situation, however, one polysiloxane in the reaction will comprise one reactive group and the second polysiloxane will comprise a second reactive group which reacts with the first.
• the organosilicon material comprises a chain extension agent
• it can be a material such as a silane, a siloxane (e.g., disiloxane or trisiloxane) or a silazane.
• a composition comprising a polysiloxane according to the above structure (I) which has at least one Si-OH group can be chain extended by using an alkoxysilane (e.g., a dialkoxysilane or trialkoxysilane) in the presence of a tin or titanium containing catalyst.
• an alkoxysilane e.g., a dialkoxysilane or trialkoxysilane
• the metal containing catalysts used in the above chain extension reactions are often specific to the particular reaction. Such catalysts, however, are known in the art. Generally, they are materials containing metals such as platinum, rhodium, tin, titanium, copper, lead, etc.
• the polysiloxane has at least one aliphatically unsaturated group, preferably an end group
• the organosilicon material is a siloxane or a polysiloxane having at least one Si-H group, preferably an end group, in the presence of a hydrosilylation catalyst.
• the polysiloxane having at least one aliphatically unsaturated group has the structure (I) wherein R, R' and n are as defined above and provided that on average between one and two (inclusive) R or R' groups comprise an aliphatically unsaturated group per polymer.
• the organosilicon material having at least one Si-H group preferably has the above structure (I) wherein R, R' and n are as defined above and provided that on average between one and two (inclusive) R or R' groups comprise hydrogen atoms and n is 0 or a positive integer.
• This material can be a polymer or a lower molecular weight material such as a siloxane (e.g., a disiloxane or a trisiloxane).
• the polysiloxane having at least one aliphatically unsaturated group and the organosilicon material having at least one Si-H group react in the presence of a hydrosilylation catalyst.
• a hydrosilylation catalyst Such catalysts are known in the art and can include, for example, platinum and rhodium containing materials. These catalysts may take any of the known forms such as platinum or rhodium deposited on carriers such as silica gel or powdered charcoal, or other appropriate compounds such as platinic chloride, salts of platinum and chloroplatinic acids.
• a preferred material is chloroplatinic acid either as the commonly obtainable hexahydrate or the anhydrous form because of its easy dispersibility in organosilicon systems and its non-effect on colour of the mixture.
• Platinum or rhodium complexes may also be used e.g. those prepared from chloroplatinic acid hexahydrate and divinyltetramethyldisiloxane. Generally, these catalysts are used in amounts of between about 0.0001 and 10 wt. % based on the weight of the composition (I).
• the polysiloxane has at least one Si-OH group, preferably an end group, and the organosilicon material has at least one alkoxy group, preferably a siloxane having at least one Si-OR group, or an alkoxysilane having at least two alkoxy groups in the presence of a metal containing catalyst.
• the polysiloxane having at least one SiOH group has the structure (I) wherein R, R' and n are as defined above and on average between one and two (inclusive) R or R' groups comprise a hydroxyl group (OH).
• the organosilicon material having at least one alkoxy group can have the structure (I) wherein R, R' and n are as defined above and on average between one and two (inclusive) R or R' groups comprise alkoxy groups, e.g., of the structure (OR) in which R is as defined above and n is 0 or a positive integer.
• the organosilicon material can be a silane of the structure R m Si(OR) 4-m, wherein R is as defined above and m is 0 to 2.
• Other materials containing the alkoxy group e.g., alkoxy- alkoxys may also be used herein.
• metal catalysts for the reaction of an Si-OH with an Si-OR are known in the art and may be employed including, for example, organic metal compounds such as organotin salts, titanates, or titanium chelates or complexes.
• organic metal compounds such as organotin salts, titanates, or titanium chelates or complexes.
• catalysts include stannous octoate, dibutyltin dilaurate, dibutyltin diacetate, dimethyltin dineodecanoate, dibutyltin dimethoxide, isobutyl tin triceroate, dimethyltin dibutyrate, dimethyltin dineodecanoate, triethyltin tartrate, tin oleate, tin naphthenate, tin butyrate, tin acetate, tin benzoate, tin sebacate, tin succinate, tetrabutyl titanate, tetraiso
• any composition containing at least one polysiloxane, at least one organosilicon material that reacts with said polysiloxane by a chain extension reaction and a metal containing catalyst for said chain extension reaction can be used herein.
• the mixture used to form the emulsion also contains at least one surfactant (II).
• This can be a non-ionic surfactant, a cationic surfactant, an anionic surfactant, alkylpolysaccharides, amphoteric surfactants and the like.
• non-ionic surfactants include polyoxyalkylene alkyl ethers, polyoxyalkeylene sorbitan alkyl esters, polyoxyalkylene alkyl esters, and polyoxyalkylene alkylphenol ethers, polyethylene glycols, polypropylene glycols, and diethylene glycols.
• cationic surfactants include quaternary ammonium hydroxides such as tetramethylammonium hydroxide, octyltrimethylammonium hydroxide, dodecyl-trimethyl ammonium hydroxide, hexadecyltrimethyl ammonium hydroxide, octyldimethylbenzylammonium hydroxide, decyldimethylbenzyl ammonium hydroxide, didodecyldimethyl ammonium hydroxide, dioctadecyl dimethylammonium hydroxide, tallow trimethylammonium hydroxide and cocotrimethylammonium hydroxide as well as corresponding salts of these materials, fatty acid amines and amides and their derivatives and the salts of the fatty acid amines and amides including aliphatic fatty amines and their derivatives, homologs of aromatic amines having fatty chains, fatty amides derived from aliphatic diamines
• Suitable anionic surfactants include alkyl sulfates such as lauryl sulfate, polymers such as acrylates/C10-30 alkyl acrylate crosspolymer alkylbenzenesulfonic acids and salts such as hexylbenzenesulfonic acid, octylbenzenesulfonic acid, decylbenzenesulfonic acid, dodecylbenzenesulfonic acid, cetylbenzenesulfonic acid and myristylbenzenesulfonic acid; the sulfate esters of monoalkyl polyoxyethylene ethers; alkylnapthylsulfonic acid; alkali metal sulforecinates, sulfonated glyceryl esters of fatty acids such as sulfonated monoglycerides of coconut oil acids, salts of sulfonated monovalent alcohol esters, amides of amino sulfonic acids,
• alkylpolysaccharides include, for example, materials of the structure R 1 -O- (R 2 O) m - (G) n wherein R 1 represents a linear or branched alkyl group, a linear or branched alkenyl group or an alkylphenyl group, R 2 represent an alkylene group, G represents a reduced sugar, m denotes 0 or a positive integer and n represent a positive integer as described, for example, in US Patent 5,035,832.
• amphoteric surfactants include cocamidopropyl betaine and cocamidopropyl hydroxysulfate.
• the above surfactants may be used individually or in combination.
• the particle size of the silicone in the emulsion is dependent on, among other factors, the amount and type of surfactant employed.
• the amount of surfactant used will vary depending on the surfactant, but generally it is used in an amount of between about 1 and 30 wt. % based on the total weight of the composition (I).
• the final material used to form the emulsions herein is the water which forms the continuous phase of the emulsion and into which the silicone oil droplets are dispersed.
• materials which assist in the chain extension reaction e.g., other chain extenders
• conventional inhibitors perfumes, colorants, thickeners, preservatives, plasticizers, active ingredients (e.g., pharmaceuticals) and the like may be used herein.
• composition (I), surfactant (II) and water (III) are mixed by simple agitation to form a coarse water in oil mixture. This mixture is then emulsified. During emulsification, the coarse water in oil mixture is inverted into a fine silicone in water emulsion.
• the emulsification can be accomplished by conventional means such as a batch mixer, colloid mill or line mixer. The emulsification process is, thus, simple and fast.
• composition (I), surfactant (II) and water (III) can be mixed all at once or, alternatively, the materials can be mixed in any order.
• the polysiloxane, the organosilicon material and the metal containing catalyst of composition (I) are combined, the polymerisation reaction begins.
• anionic surfactants often increase the kinetics of the chain extension reaction between a polysiloxane having at least one aliphatically unsaturated group and an organosilicon material having at least one Si-H group in the presence of a hydrosilylation catalyst.
• a hydrosilylation catalyst e.g., the platinum
• a cure inhibitor could be added to control the reaction kinetics.
• the water is then added and the silicone phase inverted to form silicone droplets in the water as described above. After inversion, the chain extension reaction continues within the silicone droplet until all the materials have reacted or the reaction has been inhibited.
• the quantity of water and/or surfactant used in the initial phase inversion process may have an impact on the particle size of the final emulsion. For instance, if an emulsion is formed with the same quantity of water in two instances but in the first a large quantity of water is mixed before the phase inversion step and in the second a small quantity of water is mixed before the phase inversion step followed by mixing the remaining additional water after the phase inversion step, the first emulsion will generally have a larger particle size than the second.
• the total amount of water used is generally between about 1 and 99 wt. %, preferably between about 6 and about 99 wt. %, based on the weight of the emulsion.
• the polymerisation of the present invention takes place at the interior of the oil droplets by chain extension (i.e., not at the o/w interface) as shown by the fact that the silicone in the droplets generally have the same viscosity as if the silicone is mixed in bulk (i.e., non-emulsified).
• the degree of polymerisation is not controlled by droplet size, but by the ratio of materials used in the chain extension.
• This allows for the production of a broad range of monodisperse droplet sizes containing polysiloxanes with a high viscosity.
• this technique allow for the production of emulsions with high silicone volume fractions.
• Another of the advantages of the process of the invention is that it can be performed without heat and acidic or basic catalysts in a relatively short time using a wide range of surfactants.
• the emulsions of the present invention can generally have a silicone loading in the range of about 1 to about 94 wt. %.
• the molecular weight of the silicone can be in the range of about 1 mm 2 /sec at 25°C to in excess of 10 8 mm 2 /sec at 25°C.
• the mean particle size of the emulsion can vary from about 0.3 to in excess of 100 micrometers. Particularly relevant is the fact that this process produces previously unknown emulsions in which the mean particle size is in the range of about 0.3 micrometers and the viscosity of the silicone is greater than 10 5 mm 2 /sec. Specifically, we have discovered emulsions in which the mean particle size is in the range of about 0.3, preferably 1, to 100 micrometers with viscosities of the silicone in the range of 10 6 to 10 8 mm 2 /sec.
• the emulsions of the invention also have a number of other practical advantages.
• the emulsions of the invention render the high molecular weight silicone in the droplets easily handleable.
• the silicone in the droplets of the invention generally have the same viscosity as if the silicone is mixed in bulk, one can determine the viscosity of the silicone before emulsion. Also, this allows one to easily perform quality checks on the silicone in the emulsions.
• the emulsions of the invention are useful in the standard applications for silicone emulsions. Thus, they are useful for personal care applications such as on hair, skin, mucous, teeth, etc.
• the silicone is lubricious and will improve the properties of skin creams, skin care lotions, moisturisers, facial treatments such as acne or wrinkle removers, personal and facial cleansers, bath oils, perfumes, fragrances, colognes, sachets, sunscreens, pre-shave and after shave lotions, shaving soaps and shaving lathers. It can likewise be use in hair shampoos, hair conditioners, hair sprays, mousses, permanents, depilatories, and cuticle coats to provide conditioning benefits.
• the emulsions of this invention impart a dry silky-smooth payout.
• ком ⁇ онент When used in personal care products, they are generally incorporated in amounts of about 0.01 to about 50 weight percent, preferably 0.1 to 25 wt. percent, of the personal care product. They are added to conventional ingredients for the personal care product chosen. Thus, they can be mixed with deposition polymers, surfactants, detergents, antibacterials, anti-dandruffs, foam boosters, proteins, moisturising agents, suspending agents, opacifiers, perfumes, colouring agents, plant extracts, polymers, and other conventional care ingredients.
• deposition polymers surfactants, detergents, antibacterials, anti-dandruffs, foam boosters, proteins, moisturising agents, suspending agents, opacifiers, perfumes, colouring agents, plant extracts, polymers, and other conventional care ingredients.
• the emulsion of the invention are useful for numerous other applications such as textile fibre treatment, leather lubrication, fabric softening, release agents, water based coatings, oil drag reduction, lubrication, facilitation of cutting cellulose materials, and in many other areas where silicones are conventionally used.
• Examples 1-3 were repeated except the water was added in 2 stages in the following amounts: 7 parts and 5 parts.
• the resultant materials had mean particle sizes of 8.5 microns in each case.
• Examples 1-3 were repeated except that 12 parts water was added in 1 single stage.
• the resultant materials had mean particle sizes of 60 microns in each case.
• This example demonstrates the use of different surfactants.

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• Chemical & Material Sciences (AREA)
• Health & Medical Sciences (AREA)
• Chemical Kinetics & Catalysis (AREA)
• Medicinal Chemistry (AREA)
• Polymers & Plastics (AREA)
• Organic Chemistry (AREA)
• Dispersion Chemistry (AREA)
• Silicon Polymers (AREA)
• Compositions Of Macromolecular Compounds (AREA)
• Processes Of Treating Macromolecular Substances (AREA)

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• 1997
  • 1997-04-23 GB GBGB9708182.2A patent/GB9708182D0/en active Pending
• 1998
  • 1998-04-20 US US09/062,801 patent/US6013682A/en not_active Expired - Lifetime
  • 1998-04-22 DE DE69825521T patent/DE69825521T2/de not_active Expired - Lifetime
  • 1998-04-22 AU AU63527/98A patent/AU743951B2/en not_active Ceased
  • 1998-04-22 EP EP98303076A patent/EP0874017B1/fr not_active Expired - Lifetime
  • 1998-04-23 KR KR1019980014439A patent/KR100563747B1/ko not_active Expired - Lifetime
  • 1998-04-23 JP JP11367998A patent/JP4329948B2/ja not_active Expired - Lifetime

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